Trazodone Hydrochloride NDC 71335-3022

Product information

Brand name (proprietary)

Trazodone Hydrochloride

Generic name (nonproprietary)

trazodone hydrochloride

Active ingredients

Trazodone hydrochloride — 100 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 204852

Marketing start

Sep 15, 2015

Listing expires

Dec 31, 2026

Identifiers

Product ID 71335-3022_444e384e-55aa-4354-822b-167fcba6ea0bSPL ID 444e384e-55aa-4354-822b-167fcba6ea0bSPL set ID fdd35113-5f51-49c5-a29c-ffdddd28ef38RxCUI 856373UNII 6E8ZO8LRNM

Pharmacologic class

Serotonin Reuptake Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471335302202 followed by a unit qualifier and the quantity Copy

Package 71335-3022-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Other NDCs under ANDA 204852

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.